Synthesis and Biological Evaluation of Octahydroquinazolinones as Phospholipase A2, and Protease Inhibitors: Experimental and Theoretical Exploration

Phospholipase A2 (PLA2) promotes inflammation via lipid mediators and releases arachidonic acid (AA), and these enzymes have been found to be elevated in a variety of diseases, including rheumatoid arthritis, sepsis, and atherosclerosis. The mobilization of AA by PLA2 and subsequent synthesis of prostaglandins are regarded as critical events in inflammation. Inflammatory processes may be treated with drugs that inhibit PLA2, thereby blocking the COX and LOX pathways in the AA cascade. To address this issue, we report herein an efficient method for the synthesis of a series of octahydroquinazolinone compounds (4a–h) in the presence of the catalyst Pd-HPW/SiO2 and their phospholipase A2, as well as protease inhibitory activities. Among eight compounds, two of them exhibited overwhelming results against PLA2 and protease. By using FT-IR, Raman, NMR, and mass spectroscopy, two novel compounds were thoroughly studied. After carefully examining the SAR of the investigated compounds against these enzymes, it was found that compounds (4a, 4b) containing both electron-donating and electron-withdrawing groups on the phenyl ring exhibited higher activity than compounds with only one of these groups. DFT studies were employed to study the electronic nature and reactivity properties of the molecules by optimizing at the BLYP/cc-pVDZ. Natural bond orbitals helped to study the various electron delocalizations in the molecules, and the frontier molecular orbitals helped with the reactivity and stability parameters. The nature and extent of the expressed biological activity of the molecule were studied using molecular docking with human non-pancreatic secretory phospholipase A2 (hnps-PLA2) (PDB ID: 1DB4) and protease K (PDB ID: 2PWB). The drug-ability of the molecule has been tested using ADMET, and pharmacodynamics data have been extracted. Both the compounds qualify for ADME properties and follow Lipinski’s rule of five.


Introduction
The chemistry of heterocyclic compounds is an area of great interest for organic as well as medicinal chemists because of their tremendous applications based on their strong coordination abilities and high electron-donating nature [1]. Manipulation and deep study of the biology and chemistry of the heterocyclic moieties paved the way for the discovery of several drugs having clinical significance [2][3][4]. A newly synthesized Schiff's base containing an azo linkage was shown as a carbon steel corrosion inhibitor in 1 M H 2 SO 4 [2][3][4] and selective naked-eye sensors for acetate anion [5]. Isoenzymes of human carbonic anhydrase (hCA) contain zinc ions, and they are widespread metalloenzymes that play an important role in maintaining pH equilibrium [6].
Heterocyclic structures having a nitrogen bicyclic nucleus such as quinzolines and octahydroquinazolines are the pioneers for the development of a large number of drugs, and several researchers around the world have also focused on other studies [7]. Recently, octahydroquinazoline scaffolds have been reported with a variety of medicinal properties, including anticancer [8], anti-inflammatory [9], and antimicrobial [10]. The acid-catalyzed cyclocondensation of aldehydes, ethylacetoacetate, and urea to produce octahydroquinazoline is a well-known Bigineli type of reaction [11]. HCl, Conc. H 2 SO 4 [11], and some Lewis acids (La(OTf) [3], L 2 O 3 , ZrCl 4 ) [12] were used as catalysts in the synthesis of octahydroquinazoline. These are well-known reagents, but their usage in octahydroquinazoline synthesis is limited due to their low yield, side product generation, and relative cost. The multifunctional polyoxometalates family of acids, notably heteropoly acid (HPA), is more active than other solid acids (SiO 2 , zeolites, and Al 2 O 3 ) as a replacement for such acids [13]. Due to its poor thermal stability, HPA has a small surface area and a limited ability to regenerate. Certain transition metals (Pd/Pt) and silicon dioxide were added to HPA to improve the regeneration capacity and increase the surface area, respectively [14]. Phospholipases A2 (PLA2) are secretory enzymes that catalyze the breakdown of membrane glycerophospholipids to liberate fatty acids and lysophospholipids [15]. They are abundantly found in mammals and snake venoms. They play a role in a variety of inflammatory processes, including the production of eicosanoids and lysophospholipids, cellular membrane homeostasis, and lipid digestion [16]. PLA2 is divided into ten categories: IB, IIA, IIC, IID, IIE, IIF, III, V, X, and XIIA [17]. Among these groups, IB PLA2 has been reported to be involved in physiological and pathophysiological processes such as cell migration, proliferation, apoptosis, and hormone release [18]. In addition, PLA2 is also found in body secretions such as pancreatic juices, arthritic synovial fluid [19], and in the serum of patients suffering from lung injury [20] and chronic renal failure [21].
Proteases are proteolytic enzymes that aid in the breakdown of proteins into peptides and amino acids. These enzymes are categorized as Bacillus protease, protease-esperase, and protease K [22] based on their sources and functions. Many pathogenic disorders, such as inflammation, cancer, hypertension, and AIDS, are caused by enzymes derived from plants, animals, and microbes [18]. Protease inhibitors can thus be employed as therapeutic targets in the development of medicines and the prevention of disease. Quinazoline derivatives are being studied to see if they can eliminate the risk factors for colorectal cancer (CRC) and other inflammatory disorders by inhibiting proteases or proteases and phospholipase A2 [23][24][25].

Chemistry
As shown in Scheme 1, compounds were produced utilizing Pd-HPW/SiO2 as green catalysts in absolute aqueous conditions. As a result, only two of all synthesized compounds exhibited good biological activities. Therefore, we tested further FT-IR, Raman, mass, and NMR techniques to elucidate newly synthesized compounds spectroscopically. Scheme 1. Pd-HPW/SiO2 catalyst-mediated octahydroquinazolinone synthesis.

FT-IR
Compounds 4a and 4b were confirmed by FT-IR. The frequencies at 3477 and 3363, and 3390 and 3380 cm −1 in FT-IR symmetric stretching N-H vibrations are for compounds 4a and 4b, respectively. Peaks at 3191 and 3305 cm −1 are attributed to broad OH [26,27]. The C=O ring has a peak between 1683 and 1685 cm −1 for both compounds. For 4a and 4b, the peaks at 1593 and 1595 belong to amide (CO-NH) and thioamide (C=S-NH), respectively, indicating the synthesis of octahydroquinazolinenone. Another distinctive peak

Chemistry
As shown in Scheme 1, compounds were produced utilizing Pd-HPW/SiO 2 as green catalysts in absolute aqueous conditions. As a result, only two of all synthesized compounds exhibited good biological activities. Therefore, we tested further FT-IR, Raman, mass, and NMR techniques to elucidate newly synthesized compounds spectroscopically.

Chemistry
As shown in Scheme 1, compounds were produced utilizing Pd-HPW/SiO2 as gre catalysts in absolute aqueous conditions. As a result, only two of all synthesized co pounds exhibited good biological activities. Therefore, we tested further FT-IR, Rama mass, and NMR techniques to elucidate newly synthesized compounds spectroscopical Scheme 1. Pd-HPW/SiO2 catalyst-mediated octahydroquinazolinone synthesis.

FT-IR
Compounds 4a and 4b were confirmed by FT-IR. The frequencies at 3477 and 33 and 3390 and 3380 cm −1 in FT-IR symmetric stretching N-H vibrations are for compoun 4a and 4b, respectively. Peaks at 3191 and 3305 cm −1 are attributed to broad OH [26,2 The C=O ring has a peak between 1683 and 1685 cm −1 for both compounds. For 4a and 4 the peaks at 1593 and 1595 belong to amide (CO-NH) and thioamide (C=S-NH), resp tively, indicating the synthesis of octahydroquinazolinenone. Another distinctive pe Scheme 1. Pd-HPW/SiO 2 catalyst-mediated octahydroquinazolinone synthesis.

FT-IR
Compounds 4a and 4b were confirmed by FT-IR. The frequencies at 3477 and 3363, and 3390 and 3380 cm −1 in FT-IR symmetric stretching N-H vibrations are for compounds 4a and 4b, respectively. Peaks at 3191 and 3305 cm −1 are attributed to broad OH [26,27]. The C=O ring has a peak between 1683 and 1685 cm −1 for both compounds. For 4a and 4b, the peaks at 1593 and 1595 belong to amide (CO-NH) and thioamide (C=S-NH), respectively, indicating the synthesis of octahydroquinazolinenone. Another distinctive peak was discovered at 1419 and 1407 cm −1 , which was attributed to C=C of the required octahydroquinazolines of compounds 4a and 4b, respectively [28]. In compound 4b, there is also a C=S peak coupled with a weak symmetric N-H bending at 813 cm −1 [29]. 4

Raman Spectroscopy
The Raman spectra of compounds 4a and 4b showed a band at 1600 cm −1 attributed to C=O functional groups and a band around or above 3000 cm −1 attributed to both -NH-and phenyl OH groups, and these results were confirmed by the literature [30] as in Figure 2.
There are many small peaks in the Raman spectra between 1000 and 1500 cm −1 . In the Raman spectra, the in-plane distortion of the OH band is ascribed to 1450 cm −1 . The stretching mode of the hydroxyl groups with respect to the phenyl moiety arises around 1270 cm −1 in the Raman spectra, as expected [31]. In the Raman spectra of both of the compounds discussed, the unique C=C band was detected around 1550 cm −1 [31]. In addition, another strong band at 650 cm −1 was identified in both the Raman spectra and must be assigned to the C=O and C=S compounds, respectively, for 4a and 4b.
was discovered at 1419 and 1407 cm −1 , which was attributed to C=C of the required oc tahydroquinazolines of compounds 4a and 4b, respectively [28]. In compound 4b, there is also a C=S peak coupled with a weak symmetric N-H bending at 813 cm −1 [29].

Raman Spectroscopy
The Raman spectra of compounds 4a and 4b showed a band at 1600 cm −1 attributed to C=O functional groups and a band around or above 3000 cm −1 attributed to both -NH and phenyl OH groups, and these results were confirmed by the literature [30] as in Figure  2. There are many small peaks in the Raman spectra between 1000 and 1500 cm −1 . In the Raman spectra, the in-plane distortion of the OH band is ascribed to 1450 cm −1 . The stretching mode of the hydroxyl groups with respect to the phenyl moiety arises around 1270 cm −1 in the Raman spectra, as expected [31]. In the Raman spectra of both of the com pounds discussed, the unique C=C band was detected around 1550 cm −1 [31]. In addition another strong band at 650 cm −1 was identified in both the Raman spectra and must be assigned to the C=O and C=S compounds, respectively, for 4a and 4b.

NMR Spectrum
In the 1 H NMR spectra, the formation of the octahydroquinazolinone skeleton was clearly confirmed by the fact that the H4 methine proton of compounds 4a and 4b appeared at δ 5.03. One unreacted -OH of o-vanillin is available in both of the compounds at δ 10.37 ppm for H1, respectively.

NMR Spectrum
In the 1 H NMR spectra, the formation of the octahydroquinazolinone skeleton was clearly confirmed by the fact that the H4 methine proton of compounds 4a and 4b appeared at δ 5.03. One unreacted -OH of o-vanillin is available in both of the compounds at δ 10.37 ppm for H1, respectively.
In the 13 CNMR spectra of the compounds 4a and 4b, the most deshielded carbon atoms were located at C5 and C2. Both compounds have values of 196.2 ppm for the most deshielded carbon of C5. The second-most deshielded carbon at C2 belongs to >C=O in compound 4a, which has δ 165.8 ppm. On the other hand, in compound 4b, C2 of >C=S appeared in the spectra with an experimental value of 170.36 ppm. C=O and C=S resonances are slightly deshielded with higher chemical shifts, which may be due to intramolecular hydrogen bonding of compounds 4a and 4b and the electronegativity of oxygen and sulphur [32].
The most characteristic carbon at C4 resonates at δ 45.2 for compounds 4a and 4b at 43.50 ppm, respectively. Carbon 8a, for compounds 4a and 4b, resonates at δ 164.0 and 165.03 ppm, respectively. The signals for aromatic carbon and other primary, secondary, and tertiary carbon were displayed in the Supplementary Material ( Figures S2 and S6).
In the 13 CNMR spectra of the compounds 4a and 4b, the most deshielded carbon atoms were located at C5 and C2. Both compounds have values of 196.2 ppm for the most deshielded carbon of C5. The second-most deshielded carbon at C2 belongs to >C=O in compound 4a, which has δ 165.8 ppm. On the other hand, in compound 4b, C2 of >C=S appeared in the spectra with an experimental value of 170.36 ppm. C=O and C=S resonances are slightly deshielded with higher chemical shifts, which may be due to intramolecular hydrogen bonding of compounds 4a and 4b and the electronegativity of oxygen and sulphur [32].
The most characteristic carbon at C4 resonates at δ 45.2 for compounds 4a and 4b at 43.50 ppm, respectively. Carbon 8a, for compounds 4a and 4b, resonates at δ 164.0 and 165.03 ppm, respectively. The signals for aromatic carbon and other primary, secondary, and tertiary carbon were displayed in the Supplementary Material ( Figures S2 and S6).

Phospholipase (PLA 2 ) Inhibitory Activity
The phospholipase inhibitory activity of octahydroquinazolines 4a-h has been detected at concentrations of 0.01 to 0.08 g/L, as shown in Figure 3. PLA2 inhibitory activity (inhibition) was found to be increasing with a corresponding increase in concentration for compounds 4a-h. At a minimum concentration of 0.01 g/L, compounds 4a and 4b displayed 40.23% ± 2.41% and 38.46% ± 2.74%, while maximum activity for compounds 4a and 4b was exhibited at 92.86% ± 3.18% and 89.72% ± 3.66% at 0.05 g/L, as shown in Figure 3. For the rest of the compounds such as 4c, 4d, 4e, 4f, 4g, and 4h at each concentration, inhibitory activity against PLA2 was identified as insignificant. The results are somewhat in agreement with our previous work with the same enzyme, and the PLA 2 inhibitory efficiencies of the current molecules are found to be even better than those of other established quinazolines or other moieties [18,23,25]. Oleanolic acid acts as a reference molecule and showed relatively less potency (72.43% ± 2.79%) as compared to compounds 4a and 4b, but more than other least active compounds (4c, 4d, 4e, 4f, 4g, and 4h) at maximum concentration. By looking at the IC 50 results of compounds 4a-h, they represent moderate to high PLA2 activities, which are demonstrated in terms of ranges from 0.029-0.049 g/L. The highest significant activity belongs to compounds 4a and 4b, with IC 50 values of 0.029 and 0.030 g/L, respectively ( Table 1). The clinical significance of these compounds could be attributed to the fact that in many inflammatory conditions, PLA2 levels are elevated [33], and hence, they will be explored in such an ailment.

Phospholipase (PLA2) Inhibitory Activity
The phospholipase inhibitory activity of octahydroquinazolines 4a-h has been detected at concentrations of 0.01 to 0.08 g/L, as shown in Figure 3. PLA2 inhibitory activity (inhibition) was found to be increasing with a corresponding increase in concentration for compounds 4a-h. At a minimum concentration of 0.01 g/L, compounds 4a and 4b displayed 40.23% ± 2.41% and 38.46% ± 2.74%, while maximum activity for compounds 4a and 4b was exhibited at 92.86% ± 3.18% and 89.72% ± 3.66% at 0.05 g/L, as shown in Figure  3. For the rest of the compounds such as 4c, 4d, 4e, 4f, 4g, and 4h at each concentration, inhibitory activity against PLA2 was identified as insignificant. The results are somewhat in agreement with our previous work with the same enzyme, and the PLA2 inhibitory efficiencies of the current molecules are found to be even better than those of other established quinazolines or other moieties [18,23,25]. Oleanolic acid acts as a reference molecule and showed relatively less potency (72.43% ± 2.79%) as compared to compounds 4a and 4b, but more than other least active compounds (4c, 4d, 4e, 4f, 4g, and 4h) at maximum concentration. By looking at the IC50 results of compounds 4a-h, they represent moderate to high PLA2 activities, which are demonstrated in terms of ranges from 0.029-0.049 g/L. The highest significant activity belongs to compounds 4a and 4b, with IC50 values of 0.029 and 0.030 g/L, respectively ( Table 1). The clinical significance of these compounds could be attributed to the fact that in many inflammatory conditions, PLA2 levels are elevated [33], and hence, they will be explored in such an ailment.

Protease Activity
The synthesized octahydroquinazolinones (4a, 4b) were screened against the protease K enzyme at a concentration of 0.1 to 0.8 mg/ mL, as shown in Figure 4. Protease inhibitory activity was exhibited in a dose-dependent manner. At all concentrations, 4a and 4b displayed better activity than the rest of the tested compounds (4c, 4d, 4e, 4f, 4g, and 4h). Among these unsatisfactory compounds, the least protease inhibitory activity was observed at 0.1 mg/mL and was only 10 ± 2.14 for compound 4c and 45 ± 1.89 for compound 4e at 0.8 mg/mL. The maximum inhibition (85 ± 5.82) and (75 ± 4.66) was displayed at a concentration of 0.6 mg/mL by compounds 4a and 4b, respectively, which is better than some previous results, where protease inhibition was achieved at only 73.33% [18,24]. A protease inhibitor cocktail (Sigma) was used as the positive control, and the inhibitory potential was found to be close to maximum inhibition (83 ± 2.73). IC 50 results for compounds 4a-h for antiprotease activities demonstrated a range of 0.039-0.963 mg/L. The most promising candidates in terms of antiprotease activity were reported with IC 50 values of 0.39 and 0.037 mg/L, respectively, for compounds 4a and 4b. Other compounds with IC 50 values and their respective antiprotease activities showed moderate to good activity, as shown in Table 2. Regardless of the concentration, compound 4a was the most promising candidate against phospholipase A2 (PLA2) and protease K enzymes under trial and could be presented as a prime anti-inflammatory agent.

Protease Activity
The synthesized octahydroquinazolinones (4a, 4b) were screened against the protease K enzyme at a concentration of 0.1 to 0.8 mg/ mL, as shown in Figure 4. Protease inhibitory activity was exhibited in a dose-dependent manner. At all concentrations, 4a and 4b displayed better activity than the rest of the tested compounds (4c, 4d, 4e, 4f, 4g, and 4h). Among these unsatisfactory compounds, the least protease inhibitory activity was observed at 0.1 mg/mL and was only 10 ± 2.14 for compound 4c and 45 ± 1.89 for compound 4e at 0.8 mg/mL. The maximum inhibition (85 ± 5.82) and (75 ± 4.66) was displayed at a concentration of 0.6 mg/mL by compounds 4a and 4b, respectively, which is better than some previous results, where protease inhibition was achieved at only 73.33% [18,24]. A protease inhibitor cocktail (Sigma) was used as the positive control, and the inhibitory potential was found to be close to maximum inhibition (83 ± 2.73). IC50 results for compounds 4a-h for antiprotease activities demonstrated a range of 0.039-0.963 mg/L. The most promising candidates in terms of antiprotease activity were reported with IC50 values of 0.39 and 0.037 mg/L, respectively, for compounds 4a and 4b. Other compounds with IC50 values and their respective antiprotease activities showed moderate to good activity, as shown in Table 2. Regardless of the concentration, compound 4a was the most promising candidate against phospholipase A2 (PLA2) and protease K enzymes under trial and could be presented as a prime anti-inflammatory agent.  The condensation of dimedone (1), urea/thiourea (2), and substituted aldehydes (3a-h) yielded a series of octahydroquinazolinone derivatives (4a-h) using 1% Pd-HPW/SiO 2 as a catalyst. Only two of the synthesized compounds (4a and 4b) showed satisfactory results in terms of inhibitory PLA2 (%) and antiprotease (%) activities. When the structureactivity relationship (SAR) was established among all tested compounds, no clear reason was revealed except a dose-dependent relationship among them. Due to the presence of electron-withdrawing (OCH 3 ) and electron-donating (OH) functional groups on their respective phenyl moieties, two of the most promising compounds, 4a and 4b, perform as the best PLA2 and antiprotease agents. Due to the fact that their phenyl moieties include either electron-withdrawing (4c, 4d, 4f, 4g) or electron-donating (4e, 4h) groups, the remaining compounds do not exhibit any discernible enzymatic activity.   Tables S1 and S2 show the Cartesian coordination and physical parameters of molecules 4a and 4b, respectively. Figure 5 shows the geometry of molecules 4a and 4b. From Table S2, notable Table 3 shows the chemical reactivity and stability, and Figure 6 shows the frontier molecular orbitals of molecules 4a and 4b explained by some chemical descriptors. The electrophiles attack the sites of the highest occupied molecular orbital (HOMO) of molecule 4a, spreading over the 3-methoxy-2-hydroxyphenyl group. In the case of molecule 4b, it is spread over sulphur in the octahydroquinazolinone group, and the energies are −8.6269 and −7.5015 eV, respectively. The nucleophile attack sites of the lowest unoccupied molecular orbital (LUMO) of molecule 4a are spread over the octahydroquinazolinone group, and those of molecule 4b are spread over sulphur with the octahydroquinazolinone group, and the energies are −5.2689 and −5.3187 eV, respectively. The energy gap, which means electrons transfer from the valance band to the conduction band of molecules 4a and 4b, is −3.358 and −2.1828 eV, respectively, and this amount of energy  Table 3 shows the chemical reactivity and stability, and Figure 6 shows the frontier molecular orbitals of molecules 4a and 4b explained by some chemical descriptors. The electrophiles attack the sites of the highest occupied molecular orbital (HOMO) of molecule 4a, spreading over the 3-methoxy-2-hydroxyphenyl group. In the case of molecule 4b, it is spread over sulphur in the octahydroquinazolinone group, and the energies are −8.6269 and −7.5015 eV, respectively. The nucleophile attack sites of the lowest unoccupied molecular orbital (LUMO) of molecule 4a are spread over the octahydroquinazolinone group, and those of molecule 4b are spread over sulphur with the octahydroquinazolinone group, and the energies are −5.2689 and −5.3187 eV, respectively. The energy gap, which means electrons transfer from the valance band to the conduction band of molecules 4a and 4b, is −3.358 and −2.1828 eV, respectively, and this amount of energy is required for electron transitions. The smallest possible energies required for molecules 4a and 4b to form a cationic molecule are 8.62693 and 7.50153 eV, and these energies are known as ionization energies of corresponding molecules; similarly, the total amount of releasing energies required for molecules 4a and 4b to form an anionic molecule is 5.26894 and 5.31874 eV, which is also known as electron affinity of these molecules. All the molecular electrons can be stable at a particular energy point, which is mentioned as the hardness of molecules 4a and 4b at 1.67899 and 1.09139 eV, respectively; on the contrary, the energies 0.8395 and 0.5457 eV of molecules 4a and 4b electrons are unstable, which is called the softness of corresponding molecules. The total energies of molecules 4a and 4b are −6.9479 and −6.4101 eV, respectively; this is called the chemical potential energy of those molecules. When bonded electrons attract themselves, 6.94794 and 6.41013 eV of molecules 4a and 4b are required, indicating the electronegativity of the respective molecules. The amount of energies required for the addition of electrophiles to molecules 4a and 4b, respectively, is 14.3758 and 18.8245 eV, and this is known as the electrophilicity index; similarly, the amount of energies required for the addition of nucleophiles to corresponding molecules is 0.06956 and 0.05312 eV, and this is known as the nucleophilicity index. The energies 4.1337 and 6.48002 eV of molecules 4a and 4b are referred to as electron-accepting power, while the energies 11.0816 and 12.8901 eV of corresponding molecules are referred to as electron-donating power.

Frontier Molecular Orbital (FMO) Analysis of Compounds 4a and 4b
Molecules 2023, 28, x FOR PEER REVIEW 10 of 22 is required for electron transitions. The smallest possible energies required for molecules 4a and 4b to form a cationic molecule are 8.62693 and 7.50153 eV, and these energies are known as ionization energies of corresponding molecules; similarly, the total amount of releasing energies required for molecules 4a and 4b to form an anionic molecule is 5.26894 and 5.31874 eV, which is also known as electron affinity of these molecules. All the molecular electrons can be stable at a particular energy point, which is mentioned as the hardness of molecules 4a and 4b at 1.67899 and 1.09139 eV, respectively; on the contrary, the energies 0.8395 and 0.5457 eV of molecules 4a and 4b electrons are unstable, which is called the softness of corresponding molecules. The total energies of molecules 4a and 4b are −6.9479 and −6.4101 eV, respectively; this is called the chemical potential energy of those molecules. When bonded electrons attract themselves, 6.94794 and 6.41013 eV of molecules 4a and 4b are required, indicating the electronegativity of the respective molecules. The amount of energies required for the addition of electrophiles to molecules 4a and 4b, respectively, is 14.3758 and 18.8245 eV, and this is known as the electrophilicity index; similarly, the amount of energies required for the addition of nucleophiles to corresponding molecules is 0.06956 and 0.05312 eV, and this is known as the nucleophilicity index. The energies 4.1337 and 6.48002 eV of molecules 4a and 4b are referred to as electron-accepting power, while the energies 11.0816 and 12.8901 eV of corresponding molecules are referred to as electron-donating power.

Average Localized Ionization Energy (ALIE) of Molecules 4a and 4b
The average localized ionization energy (ALIE) study predicts the local ionization energy required for the electronic excitations, which is a wave function-based property, determined using the multi-wave function software with the help of the optimized geometry. Figure 7 represents the ALIE profile of the two compounds under study, which can be represented as a colored region from blue to red with scale values between 0.00 and 2.00, and the −12.50 to 12.50 Bohr 3 volume range. Blueish-green indicates the delocalization of electrons in 4a at 3-methoxy-2-hydroxylphenyl, oxygen, and nitrogen atoms in the azolin ring in quinazoline-dione groups, and in 4b at 3-methoxy-2-hydroxylphenyl, sulphur, oxygen, and nitrogen atoms in the azolin ring in quinazoline-dione groups. The blue color indicates the sigma bond and the stable bond between atoms in the molecule. The sites are from protons and carbons and lone pairs of electrons in sulphur, oxygen, and nitrogen atoms.
2.00, and the −12.50 to 12.50 Bohr 3 volume range. Blueish-green indicates the delocalization of electrons in 4a at 3-methoxy-2-hydroxylphenyl, oxygen, and nitrogen atoms in the azolin ring in quinazoline-dione groups, and in 4b at 3-methoxy-2-hydroxylphenyl, sulphur, oxygen, and nitrogen atoms in the azolin ring in quinazoline-dione groups. The blue color indicates the sigma bond and the stable bond between atoms in the molecule. The sites are from protons and carbons and lone pairs of electrons in sulphur, oxygen, and nitrogen atoms.

Molecular Electrostatic Potentials (MESP) from Electronic Charges and Nuclear Charges of Compounds 4a and 4b
Electrostatic potential can give an idea of the 3D charge distribution of the molecules, which helps to identify the possible electrophilic and nucleophilic centers. This potential can arise from electrons as well as nuclear charge. Figure 8 shows the MESP of the compounds due to electronic charges. The compounds show a color range from blue to red with scale values from −0.10 to 0.10 and from −12.45 to 12.45 in the Bohr 3 range. Molecule 4a has a blue color on all the nitrogen atoms of the octahydroquinazolinone group and the oxygen atoms of CH3O and OH in the 3-methoxy-2-hydroxylphenyl and carbonyl octahydroquinazolinone groups. These are electron-rich sites, so electrophiles can quickly attack. The red color is at carbon atoms which form a sigma bond with hydrogen atoms in the entire molecule, and they are electron-deficient sites; thus, nucleophiles can quickly attack these sites; and 4b, which has the blue color, has all of the nitrogen atoms present at the octahydroquinazolinone group, oxygen atoms at methoxy-hydroxyl in 3-methoxy-2-hydroxylphenyl and carbonyl in octahydroquinazolinone groups, and sulphur in the octahydroquinazolinone group, these are electron-rich sites, so electrophiles can quickly attack these sites. The red color on all the carbon atoms forms a sigma bond with hydrogen atoms on the whole; these are electron-poor sites, so nucleophiles can quickly attack these sites.

Molecular Electrostatic Potentials (MESP) from Electronic Charges and Nuclear Charges of Compounds 4a and 4b
Electrostatic potential can give an idea of the 3D charge distribution of the molecules, which helps to identify the possible electrophilic and nucleophilic centers. This potential can arise from electrons as well as nuclear charge. Figure 8 shows the MESP of the compounds due to electronic charges. The compounds show a color range from blue to red with scale values from −0.10 to 0.10 and from −12.45 to 12.45 in the Bohr 3 range. Molecule 4a has a blue color on all the nitrogen atoms of the octahydroquinazolinone group and the oxygen atoms of CH 3 O and OH in the 3-methoxy-2-hydroxylphenyl and carbonyl octahydroquinazolinone groups. These are electron-rich sites, so electrophiles can quickly attack. The red color is at carbon atoms which form a sigma bond with hydrogen atoms in the entire molecule, and they are electron-deficient sites; thus, nucleophiles can quickly attack these sites; and 4b, which has the blue color, has all of the nitrogen atoms present at the octahydroquinazolinone group, oxygen atoms at methoxy-hydroxyl in 3methoxy-2-hydroxylphenyl and carbonyl in octahydroquinazolinone groups, and sulphur in the octahydroquinazolinone group, these are electron-rich sites, so electrophiles can quickly attack these sites. The red color on all the carbon atoms forms a sigma bond with hydrogen atoms on the whole; these are electron-poor sites, so nucleophiles can quickly attack these sites.

Molecular Docking
Molecular docking was performed to confirm the compound's experimental biological activity and find the exact mechanism of action [37,38]. Structure-activity relationship (SAR) is an approach designed to find relationships between the chemical structure (or structurally related properties) and the biological activity (or target property) of the studied compounds. Pyrrole derivative compounds are potent inhibitors of human non-pan-

Molecular Docking
Molecular docking was performed to confirm the compound's experimental biological activity and find the exact mechanism of action [37,38]. Structure-activity relationship (SAR) is an approach designed to find relationships between the chemical structure (or structurally related properties) and the biological activity (or target property) of the studied compounds. Pyrrole derivative compounds are potent inhibitors of human non-pancreatic secretory phospholipase A2 (hnps-PLA 2 ) enzyme activity.
The molecular surface area as well as solvent accessibilities of protein (PDB ID: 1DB4) with molecules 4a and 4b are 2038.77 and 3179 (Å) 2 , while protein (PDB ID: 2PWB) with molecules 4a and 4b are 2355.89 and 2534.51 (Å) 2 , respectively. These solvent accessibilities will explain the surface area interactions between ligands and protein pockets (size and number of residues). Table 5 displays the docking score between proteins (PDB ID: 1DB4) and molecules 4a and 4b, which are 7.80 and 7.30 kcal/mol, respectively, and explains by modes the distributions from root-mean-square deviation from the upper lobe and the distributions from root-mean-square deviation from the lower lobe. Table 6 provides the details of the nature of the interaction between the drug and the protein.  Figure 9 and Figure 10 show docking interactions between molecules 4a and 4b and proteins with PDB IDs 1DB4 and 2PWB, respectively.   Table S4 illustrates the non-bond and unsatisfied bonds of molecules 4a and 4b with proteins (PDB ID: 1DB4 and 2PWB), and also explains bond distances, categories, types, and chemistry. The protein PDB ID: 1DB4 with 4a has four conventional hydrogen bonds, one pi-sigma bond, and two alkyl-alkyl bonds. In the same way, protein PDB ID: 1DB4 with 4b has three conventional hydrogen bonds, two carbon-hydrogen bonds, one pi-sulfur bond, one pi-pi T-shaped bond, and an alkyl-alkyl bond, respectively. The protein PDB ID: 2PWB with 4a has five conventional hydrogen bonds, two carbon-hydrogen bonds, one pi-cation; pi-donor hydrogen bond, and one alkyl-alkyl bond. Similarly, protein PDB ID: 2PWB with 4b has five conventional hydrogen bonds, three carbon-hydrogen bonds, and one alkyl-alkyl bond, respectively. The unsatisfied sites within molecules 4a and 4b interact with proteins PDB ID: 1DB4 and 2PWB; hydrogen and sulphur are behaving as donors, and oxygen is an acceptor.
Among these results, at a zero relative mean standard deviation (rmsd) value for both the upper and lower bases, molecule 4a has shown interactions with five different protein residues. In the same way, molecule 4b has shown interactions with eight and five different protein residues.
The ADME parameters were predicted with the Swiss ADME software. None of the compounds violated Lipinski's rule of five [39]. All the compounds (4a-b) were found to have sufficient lipophilicity for better absorption from the GIT, as shown in Figure 11. The ADME prediction profile is given in Table 7. The toxicity of the compounds was predicted using the ProTox II software, and both compounds were found to be non-toxic, with no hepatotoxicity, mutagenicity, carcinogenicity, immunotoxicity, or cytotoxicity predicted.  Table S4 illustrates the non-bond and unsatisfied bonds of molecules 4a and 4b with proteins (PDB ID: 1DB4 and 2PWB), and also explains bond distances, categories, types, and chemistry. The protein PDB ID: 1DB4 with 4a has four conventional hydrogen bonds, one pi-sigma bond, and two alkyl-alkyl bonds. In the same way, protein PDB ID: 1DB4 with 4b has three conventional hydrogen bonds, two carbon-hydrogen bonds, one pisulfur bond, one pi-pi T-shaped bond, and an alkyl-alkyl bond, respectively. The protein PDB ID: 2PWB with 4a has five conventional hydrogen bonds, two carbon-hydrogen bonds, one pi-cation; pi-donor hydrogen bond, and one alkyl-alkyl bond. Similarly, protein PDB ID: 2PWB with 4b has five conventional hydrogen bonds, three carbon-hydrogen bonds, and one alkyl-alkyl bond, respectively. The unsatisfied sites within molecules 4a and 4b interact with proteins PDB ID: 1DB4 and 2PWB; hydrogen and sulphur are behaving as donors, and oxygen is an acceptor.
Among these results, at a zero relative mean standard deviation (rmsd) value for both the upper and lower bases, molecule 4a has shown interactions with five different protein residues. In the same way, molecule 4b has shown interactions with eight and five different protein residues.
The ADME parameters were predicted with the Swiss ADME software. None of the compounds violated Lipinski's rule of five [39]. All the compounds (4a-b) were found to have sufficient lipophilicity for better absorption from the GIT, as shown in Figure 11. The ADME prediction profile is given in Table 7. The toxicity of the compounds was predicted using the ProTox II software, and both compounds were found to be non-toxic, with no hepatotoxicity, mutagenicity, carcinogenicity, immunotoxicity, or cytotoxicity predicted.
Showed the compound is devoid of any predicted toxicity. Figure 11. The bioavailability radar plots and boiled-egg graphs for the compounds 4a and 4b using Swiss ADME software.  Figure 11. The bioavailability radar plots and boiled-egg graphs for the compounds 4a and 4b using Swiss ADME software. Table 7. ADME and toxicity prediction of compounds (4a-b).

Parameters Compounds 4a 4b
validate using another algorithm. Another reason for not validating the results is that the docking results are supported by experimental evidence.

ADME Studies
The ADME parameters for compounds 4a and 4b were predicted with the SwissADME server [58].

Inhibitory Activity of Phospholipase (PLA2) Enzyme
The test of PLA2 inhibitory activity was performed as discussed before by De Arajo and Radvanybm [59]. Commercially available phospholipase A2 procured from Sigma-Aldrich (Saint Louis, MO, USA) (P6534), was used in this assay. In 100 mL H 2 O, the substrate was made up of 3.5 mM lecithin, 3 mM NaTDC, 100 mM NaCl, 10 mM CaCl 2 , and 0.055 mM red phenol as a colorimetric indicator. Phosphate buffer was used to adjust the pH of the reaction mixture to 7.6. The sPLA2 protein was solubilized in 10% acetonitrile at a concentration of 0.01 to 0.08 g/L. For 20 min at room temperature, a volume of 10 L of these PLA2 solutions was incubated with a volume of 10 L containing 10 g of each compound. After that, 1 mL of PLA2 substrate was added, and the hydrolysis kinetics was monitored for 5 min by monitoring the optical density at 558 nm. The percentage of inhibition was estimated by comparing the results to a control experiment (devoid of compound). Oleanolic acid was used as a positive control in this experiment.

Protease Inhibitory Activity
Protease K, obtained from commercially available sources (P2308, Sigma-Aldrich, Saint Louis, MO, USA), was used in this study. Briefly, protease tests were performed using Hammerstein casein as the substrate using the Kunitzcaseinolytic technique [60]. Protease inhibitory activities were measured under the same conditions, with the inhibitor (0.1 mg/mL) added to the reaction mixture and a 10 min pre-incubation at 37 • C. Following the remaining enzyme activity assay, 2 mL of 1% casein was added, and the mixture was allowed to stand for 30 min at 37 • C. The addition of 2.5 mL of a 5% TCA solution stopped the reaction. The absorbance of the reaction mixture was measured at 280 nm after centrifugation (12,000 rpm, 15 min). The amount of protease inhibitor that suppresses one unit of corresponding enzyme activity is known as a protease inhibitor unit. Along with the test, appropriate blanks for the enzyme, inhibitor, and substrate were run in parallel assays. A protease inhibitor cocktail (Sigma) was used as a positive control.

Conclusions
Herein, we reported the synthesis of a series of eight compounds and evaluated them for antiphospholipase (PLA2) and protease inhibitory activities. Among these two compounds, significant biological activities were observed against enzymes. Infrared spectroscopy, Raman, NMR, and mass spectroscopy techniques were used to characterize the novel molecules (4a, 4b). Molecular docking simulation confirmed the observed biological activity of the two compounds, with 4a having a higher docking score than 4b: −7.80 and −7.30 kcal/mol with 1DB4 and −7.00 and −6.60 kcal/mol with 2PWB, which indicate strong interactions. The compound is found to contain delocalized electrons, which affect the stability of the molecule, which is further confirmed by the stability and reactivity parameters. From the FMO analysis, 4a has a larger energy gap (∆E) than 4b, whose values are −3.3580 and −2.1828 eV, respectively. The wave function properties, such as ALIE and MESP, of both electronic and nuclear charges are shown at the reactive sites. Because molecule 4b has greater solvent accessibility for each protein than molecule 4a, there are more interactions between molecules and protein residues.  Table S1: Cartesian coordination of molecules 4a and 4b; Table S2: Physical parameters of molecules 4a and 4b; Table S3: Natural atomic orbital occupancies of molecules 4a and 4b; Table S4: Non-bond interactions of molecules (4a and 4b) with proteins (PDB IDs: 1DB4 and 2PWB).